Colon Cancer: Gene >> SEC24C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73760122:73760122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586C>T
AA Mutation	p.His196Tyr(p.H196Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73769462:73769462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2540T>A
AA Mutation	p.Leu847His(p.L847H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73768880:73768880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762092841
CDS Mutation	c.2252C>T
AA Mutation	p.Ala751Val(p.A751V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73769031:73769031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2303G>C
AA Mutation	p.Gly768Ala(p.G768A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73760758:73760758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896C>A
AA Mutation	p.Pro299His(p.P299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73767993:73767993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2167T>A
AA Mutation	p.Tyr723Asn(p.Y723N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73765554:73765554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331G>A
AA Mutation	p.Arg444His(p.R444H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339365
Start	73766407:73766407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339365
Start	73769029:73769029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2301T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339365
Start	73765804:73765804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339365
Start	73760179:73760179(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.647delC
AA Mutation	p.Pro216GlnfsTer11(p.P216Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000339365
Start	73770751:73770751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3097C>T
AA Mutation	p.Arg1033Ter(p.R1033*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000339365
Start	73765801:73765802(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764652839
CDS Mutation	c.1375dupC
AA Mutation	p.Gln459ProfsTer17(p.Q459Pfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SEC24C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73770787:73770787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756251861
CDS Mutation	c.3133C>T
AA Mutation	p.Arg1045Trp(p.R1045W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339365
Start	73769441:73769441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2519G>A
AA Mutation	p.Arg840Gln(p.R840Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript